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HRID 38042作成日:2026年10月27日
3-Nitrobenzenesulfonyl chloride → (2S,4R)-4-(3-Nitro-benzenesulfonyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester
https://huagongshe.com/reaction/38042
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 3-Nitrobenzenesulfonyl chloride | HCID 8476 | — |
| 反応物 | (2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester | HCID 2734883 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (2S,4R)-4-(3-Nitro-benzenesulfonyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester | HCID 86664754 | 103.1% |
反応手順
(2S,4R)-4-Hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (5.0 g) was dissolved in DCM (50 mL) and 3-nitrobenzenesulfonyl chloride (4.8 g) was added. This solution was cooled to 5° C. and the TEA (8.52 mL) was carefully added. The reaction mixture was stirred at 25° C. for 18 h. The reaction mixture was then extracted with 0.1 N aqueous HCl (50 mL) and aqueous Na2CO3 (50 mL) and brine (50 mL). The organic layer was dried over Na2SO4, filtrated and evaporated to dryness to yield a light brown amorphous solid (9.05 g). MS: m/z=431.4 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524710B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-ed6f79568ea1451898ce3a8046113a50 |
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| 出典メモ | uspto-grants-2013_09 |
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